SCLC Flashcards
non-smoker SCLC?
only 2-3% of cases. 98% from smoking. would re-biopsy and re-review if no smoking history
IHC markers
CD56, chromogranin, synaptophysin
TTF-1 in SCLC
positive in 70-80% cases
SCLC molecular
> 90% mutated for p53, Rb; diversity of genetic alterations with chromosomal instability
SCLC transformation
acquired resistance to EGFR TKI–> sensitizing mutation Exon 19 is retained but becomes SCLC, tx with EP
SCLC clinical
bone pain, SVC, paraneoplastic
paraneoplastic
cushing’s (5% of patients), SIADH, hypercalcemia (rare, mediated by PTHrP),
low Na at presentation
adverse prognostic factors, Tx chemo, ketoconazole, mitotane, adrenalectomy
SIADH in SCLC
10% of SCLC patients, symptoms in only half; Tx chemotherapy, fluid restrict, tolvaptan (oral V2 antagonist)
neurologic paraneoplastic
encephalomyelitis (anti-HU), retinopathy, lambart-eaton (ca channel mediated)
paraneoplastic
not effective treatments
lambert eaton syndrome
5% SCLC; proximal weakness improves with use; hyporeflexia, autonomic dysfcn, Tx IVIG, rituxan, plasmaphoresis
staging
30% with limited disease- found within one irradiation portal (can include a supraclav node); 70% extensive stage
survival
limited stage: 20mo survival, 20% cure; extensive: 10mo survival, no cure; untreated 2-4mo
treatment limited stage
concurrent chemorad better over chemo alone: sequential tx no benefit!
concurrent chemoRT
twice daily RT improved OS compared to once daily; standard of care. ongoing study to evaluate 45 v. 60Gy